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DNA Deoxyribose Nucleic Acid

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DNA Deoxyribose Nucleic Acid DNA DNA Components of DNA COMPONENTS DNA Replication DNA REPLICATION TAKES PLACE IN THE NUCLEUS END PRODUCT IS TWO IDENTICAL STRANDS ... – PowerPoint PPT presentation

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Title: DNA Deoxyribose Nucleic Acid


1
DNADeoxyribose Nucleic Acid
The Thread of Life
2
DNA
  • DNA is a double helix.
  • A bonds to T C bonds to G
  • In man, the DNA molecule , if fully extended,
    would have a total length of 1.7 metres. If you
    unwrap all the DNA you have in all your cells,
    you could reach the moon ...6000 times!

3
DNA
  • DNA STRUCTURE
  • DNA REPLICATION

4
Components of DNA
  • NUCLEOTIDE
  • Phosphate group-phosphodiester bond
  • 5-Carbon sugar-deoxyribose
  • nucleic acid (1 of the nucleic acids)
  • Guanine-Purine
  • Cytosine-Pyrimidines
  • Adenine-Purine
  • Thymine-Pyrimidines
  • Held by hydrogen bonds
  • One end of chain with free 5 phosphate group
  • Other end of chain with free 3 hydroxyl group
  • Adenine, thymine form two bonds
  • Guanine, cytosine form three bonds

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COMPONENTS
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DNA Replication
  • DNA is opened by enzymes (unzips) helicase
  • Complementary nucleotides bond with the old
    strands-
  • 2 strands created ½ is the old strand ½ is the
    new strand.

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DNA REPLICATION
  • TAKES PLACE IN THE NUCLEUS
  • END PRODUCT IS TWO IDENTICAL STRANDS
  • DURING CELL DIVISION- ONE STRAND
  • FOR EACH CELL
  • Replication occurs only in 5(P) to 3(OH)
    direction(DNA IS READ 3 to 5)
  • a. Replication of leading strand, 3' to 5' strand
  • 1. New strand grows from 5' to 3end
  • 2. Elongates towards replication fork

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REPLICATION
ENZYMES Helicase DNA polymerase Topoisomerase RNA
primer ligase
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From Genotype to Phenotype
  • Protein synthesis--converting the genetic code
    (in DNA) into proteins that the body uses
  • 3 Steps involved
  • Transcription
  • RNA splicing
  • Translation

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DNA----RNA
  • DNA
  • DOUBLE STRANDED
  • DEOXYRIBOSE
  • NUCLEIC BASES
  • THYMINE
  • GUANINE
  • ADENINE
  • CYTOSINE
  • RNA
  • SINGLE STRANDED
  • RIBOSE
  • NUCLEIC BASES
  • URACIL
  • GUANINE
  • ADENINE
  • CYTOSINE

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  • RNA
  • Differences from DNA
  • Single stranded (vs. Double stranded DNA)
  • Contains uracil in place of thymine
  • Ribose sugar (instead of deoxyribose)
  • 4 Types of RNA
  • preMRNA---transcribes the message from the
    DNA(rough blueprint)
  • mRNA (messenger RNA)-carries message to to
    ribosome(final blueprint)
  • rRNA (ribosomal RNA)--makes up the
    ribosome(forman that assembles parts of protein
    in a specific order)
  • tRNA(transfer RNA)--carries amino acids to
    ribosomes

27
tRNA
  • Anticodon of MRNA
  • Wobble to take in all possible aa combinations of
    3 nitrogen bases
  • Carries specific aa on 3 on of strand

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DNA TRANSCRIPTIONDNA- GIVES CODE TO preRNA or
hnRNA
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PROCESSING
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RIBOSOME STRUCTURE
  • A site - attracts Trna
  • P site - forms peptide bonds between aa of
    protein
  • E site - where Trns leave ribosome and aa chain
    elongates
  • 5 end with initiator sequence attaches to small
    subunit
  • Large subunit goes over small at the A site.
  • Attracts 1st Trna with aa Met

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DNA TRANSLATIONtRNA translates mRNA into proteins
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SUMMARY
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Comparison of DNA and RNA
  • RNA is single stranded
  • RNA has uracil instead of thymine
  • A-U
  • DNA is double stranded
  • DNA has thymine instead of uracil
  • A-T

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Understanding DNA
  • Inheritance/ Genetic Counseling
  • Cell function/protein synthesis
  • Embryonic development/gene regulation
  • Evolution/ phylogenetic relationships
  • Medicine/genetic diseases
  • Genetic engineering/ recombinant DNA

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Changes in Chromosomes
  • Mutation--a change in the sequence of DNA
    nucleotides (nitrogen bases)
  • Causes a change in the protein formed
  • Causes a change in organisms phenotype (trait)
  • Effects of mutations?
  • Some have little or no effect
  • A few are beneficial
  • Most are harmful or lethal (fatal)

44
Chromosomal Mutations
  • Deletion mutation--piece of chromosome breaks off
    and is lost the new DNA strands are also missing
    a piece
  • Duplication--piece of chromosome breaks off and
    is inserted on homologous chromosome
  • Translocation--piece of chromosome breaks off and
    attaches to a different, non-homologous
    chromosome
  • Inversion--piece of chromosome breaks off, turns
    around and reattaches in opposite direction

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Mutations Illustrated
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Gene mutations
  • Frameshift mutation--deletion or addition of
    single (or few) nucleotides alters the amino acid
    sequence of the protein
  • Point (Substitution) mutation--wrong base is
    added in a position--new DNA chains will show the
    change

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Point Mutations
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MUTATIONS
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Frameshift Mutations
  • Expansions are responsible for many genetic
    diseases
  • Muscular Dystrophy (CTG repeats)
  • Huntingtons (CAG repeats)
  • Fragile X (CCG repeats)

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Replication Errors and Mutations
  • Inheritance of mutations
  • Harmful mutations
  • Individuals may not live to reproductive age
  • Individuals may not develop/adapt as well
  • Advantageous mutations
  • Help survival of organism and are passed down if
    mutation occurred in cells that produce gametes

59
Genes and cancer
  • Cancer is uncontrolled, abnormal cell division
  • Apoptosis--programmed cell death, which is
    necessary for normal functioning
  • Cause of cancer?
  • Genes that control production of new cells dont
    turn off

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Genetic causes of cancer
  • Oncogenes--cause cell to become cancerous
  • Genes become oncogenes in 3 ways
  • Mutation can occur in a growth-factor gene,
    causing rapid, uncontrolled cell growth
  • Error in DNA replication, producing multiple
    copies of a single-growth factor gene
  • Change in genes location--falls under the
    control of a different promoter is transcribed
    more often (producing more growth-factor)

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Tumor suppression
  • Humans have tumor-suppressor genes which are
    natural anti-oncogenes
  • If tumor suppressor gene is mutated, uncontrolled
    growth/reproduction occurs
  • Retinoblastoma--inheritable cancer in eyes caused
    by changes in tumor-suppressor gene on chromosome
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  • Can also occur when mutations occur in an
    individual (not always inherited)
  • Identifying location of these genes can increase
    identification and treatment of cancer
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